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RESEARCH PRODUCT

CD1a down-regulation in primary invasive ductal breast carcinoma may predict regional lymph node invasion and patient outcome

Francesca MagnoG. La RoccaSimona CorraoRita AnzaloneS MarasàConsolato SergiGiovanni ZummoAnna M. CzarneckaFrancesca RappaL MarasàFrancesco Cappello

subject

Pathologymedicine.medical_specialtyHistologybusiness.industryCancerGeneral MedicineDendritic cellDuctal carcinomamedicine.diseasePathology and Forensic Medicinemedicine.anatomical_structureBreast cancerProgesterone receptormedicineCarcinomaskin and connective tissue diseasesAntigen-presenting cellbusinessLymph node

description

Aims: CD1a is a molecule belonging to the highlyconserved group of CD1 proteins. Its expression indendritic cells is related to the presentation of tumour-derived glycolipid antigens to T cells and, consequently,the development of a successful antitumour response.The aim was to investigate the presence of CD1a+ cellsin both primary tumours and lymph nodes (LN) ofa series of 35 invasive ductal carcinomas by bothimmunohistochemistry and reverse transcription-poly-merase chain reaction.Methods and results: CD1a antigen was more expressedin N0 than N1 breast cancer (P < 0.0001) in bothprimary lesions and LN metastases and correlatedpositively and significantly with oestrogen (ER) (P =0.0025) and progesterone (P = 0.0226) receptor (PR)status, as well as CD4+ and CD8+ T-lymphocyteinfiltration.Conclusions: This is the first report to show a linkbetween CD1a+ mononuclear cells in breast cancerand in paired LN metastases. The positive and signifi-cant correlations between the number of CD1a+ cellsand positivity of the primary tumour for ER and PRsuggest a possible role for CD1a as a prognostic markerfor breast cancer, raising the possibility that hormonereceptor-positive breast cancer patients may have abetter prognosis in the presence of greater dendritic cellinfiltration.Keywords: antitumour response, breast cancer, CD1a, dendritic cells, ductal carcinomaAbbreviations: BM, Barrett’s metaplasia; DC, dendritic cell; ER, oestrogen receptor; IDC, invasive ductal carcinoma;LN, lymph node; PCR, polymerase chain reaction; PR, progesterone receptor; RT, reverse transcriptase

https://doi.org/10.1111/j.1365-2559.2007.02919.x